A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366997



Internal ID21024550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16508868..16525543hg38UCSC Ensembl
chr3:16550375..16567050hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3816676
hg1916676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097087
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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